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Impaired function of dendritic cells in alymphoplasia (aly/aly) mice for expansion of CD25+CD4+ regulatory T cells.
Tamura, Chizuru; Nakazawa, Masatoshi; Kasahara, Masaki; Hotta, Chie; Yoshinari, Masahiro; Sato, Fumitaka; Minami, Mutsuhiko.
Afiliação
  • Tamura C; Department of Immunology, Yokohama City University School of Medicine, Yokohama, Japan.
Autoimmunity ; 39(6): 445-53, 2006 Sep.
Article em En | MEDLINE | ID: mdl-17060023
ABSTRACT
Alymphoplasia (aly/aly) mice are from a naturally occurring strain with a mutation in nuclear factor-kappa B inducing kinase (NIK). The NIK mutation causes disruption of the architecture of the thymus and spleen and aly/aly mice show decreased numbers of CD25+CD4+T cells in the spleen. For the expansion of CD25+CD4+T cells, interactions between dendritic cells (DCs) and CD25+CD4+ regulatory T cells are necessary. We investigated the ability of DCs to induce expansion of CD25+CD4+T cells. We found that DCs are reduced in the spleen of aly/aly mice, and showed low expressions of CD80, CD86 and MHC class II molecules on the surface. DCs from aly/aly mice showed decreased ability to present ovalbumin (OVA) to T cells from OVA specific TCR transgenic mice, and a decreased ability for alloantigen presentation. Further, DCs showed a decreased ability to induce expansion of CD25+CD4+T cells in vitro. Our results suggested that the impairment of DCs in aly/aly mice is responsible, at least in part, for the decreased numbers of CD25+CD4+T cells in the periphery of aly/aly mice.
Assuntos
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Base de dados: MEDLINE Assunto principal: Células Dendríticas / Antígenos CD4 / Linfócitos T Reguladores / Subunidade alfa de Receptor de Interleucina-2 / Doenças Linfáticas Limite: Animals Idioma: En Ano de publicação: 2006 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Células Dendríticas / Antígenos CD4 / Linfócitos T Reguladores / Subunidade alfa de Receptor de Interleucina-2 / Doenças Linfáticas Limite: Animals Idioma: En Ano de publicação: 2006 Tipo de documento: Article